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Hydroxyamine hydrochloride → HCID 178453351、化合物

HRID 927821
ノート
印刷プレビュー

反応式

HRID 927821 の反応式
C(=O)(O)[O-].[Na+].Cl.[NH2:7][OH:8].[C:9]([O:13][C:14](=[O:24])[NH:15][C:16]([C:22]#[N:23])([CH3:21])[CH2:17][CH:18]1[CH2:20][CH2:19]1)([CH3:12])([CH3:11])[CH3:10]>O.C(O)C>[C:9]([O:13][C:14](=[O:24])[NH:15][C:16]([C:22](=[NH:23])[NH:7][OH:8])([CH3:21])[CH2:17][CH:18]1[CH2:19][CH2:20]1)([CH3:10])([CH3:12])[CH3:11]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 443297Hydroxyamine hydrochlorideHCID 516892Sodium BicarbonateHCID 71087668(Cyano-cyclopropylmethyl-methyl-methyl)-carbamic acid tert-butyl ester

生成物 1

HCID 178453351HCID 178453351、化合物収率 66%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 962Water
溶媒

反応条件

温度
80 °C

実験手順

Sodium bicarbonate (247.52 mg, 2.94 mmol) was dissolved in water (2 mL) and hydroxylamine hydrochloride (204.747 mg, 2.94 mmol) was added. A solution of (1-cyano-2-cyclopropyl-1-methyl-ethyl)-carbamic acid tert-butyl ester (600 mg, 2.69 mmol) in ethanol (10 mL) was added thereto and the resulting reaction mixture was heated at 80° C. for 12 hours. After evaporation of solvents, the residue was dissolved with ethyl acetate (20 mL) and then filtered. The filtrate was concentrated in vacuo. The residue was purified by chromatography (silica gel, 25 g, 3:7 ethyl acetate/n-hexane) to give the title compound (450 mg, 66%) as white solid; LC-MS (UV peak area, ESI) 100%, 258.4 (M+H).

後処理

  1. customthe resulting reaction mixture
  2. customAfter evaporation of solvents
  3. dissolutionthe residue was dissolved with ethyl acetate (20 mL)
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated in vacuo
  6. customThe residue was purified by chromatography (silica gel, 25 g, 3:7 ethyl acetate/n-hexane)

出典と根拠

ORDレコード
ord-ac83339404a84460902da68a13eafd8f
出典データセット
uspto-grants-2016_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09290451B2

反応ノート

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